Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu. - Test2 - elhamkhani - TriplyDB

Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.

Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.

http://www.wikidata.org/entity/Q34039854

about

Biomarker profiling by nuclear magnetic resonance spectroscopy for the prediction of all-cause mortality: an observational study of 17,345 persons Global implementation of genomic medicine: We are not alone Linking a population biobank with national health registries-the estonian experience Genetic variants linked to education predict longevity Somatic mosaicism for copy-neutral loss of heterozygosity and DNA copy number variations in the human genome Identifying Cases of Type 2 Diabetes in Heterogeneous Data Sources: Strategy from the EMIF Project The association between lower educational attainment and depression owing to shared genetic effects? Results in ~25,000 subjects Overview of the BioBank Japan Project: Study design and profile Polymorphic variation in TPMT is the principal determinant of TPMT phenotype: A meta-analysis of three genome-wide association studies.Is the adiposity-associated FTO gene variant related to all-cause mortality independent of adiposity? Meta-analysis of data from 169,551 Caucasian adults Variants near CHRNA3/5 and APOE have age- and sex-related effects on human lifespan.Smoking-related general and cause-specific mortality in Estonia.The Influence of Age and Sex on Genetic Associations with Adult Body Size and Shape: A Large-Scale Genome-Wide Interaction Study.CDH13 promoter SNPs with pleiotropic effect on cardiometabolic parameters represent methylation QTLs.An epidemiological perspective of personalized medicine: the Estonian experience.Dominance genetic variation contributes little to the missing heritability for human complex traits.Heterozygous mutations in natriuretic peptide receptor-B (NPR2) gene as a cause of short stature.How are personality trait and profile agreement related?SCOPA and META-SCOPA: software for the analysis and aggregation of genome-wide association studies of multiple correlated phenotypes.MixFit: Methodology for Computing Ancestry-Related Genetic Scores at the Individual Level and Its Application to the Estonian and Finnish Population Studies.Pathogenic implications for autoimmune mechanisms derived by comparative eQTL analysis of CD4+ versus CD8+ T cells.Copy number variations and cognitive phenotypes in unselected populations Structural forms of the human amylase locus and their relationships to SNPs, haplotypes and obesity.Protocol for the China PEACE (Patient-centered Evaluative Assessment of Cardiac Events) Million Persons Project pilot.Cardiovascular Risk Factors and Ischemic Heart Disease: Is the Confluence of Risk Factors Greater Than the Parts? A Genetic Approach.Ultra-rare disruptive and damaging mutations influence educational attainment in the general population.Autosomal genetic control of human gene expression does not differ across the sexes.Whole-exome sequencing identifies a potential TTN mutation in a multiplex family with inguinal hernia.Demographic associations for autoantibodies in disease-free individuals of a European population.The Prevalence of PMM2-CDG in Estonia Based on Population Carrier Frequencies and Diagnosed Patients.Comparing distributions of polygenic risk scores of type 2 diabetes and coronary heart disease within different populations.The Genetic Architecture of Gene Expression in Peripheral Blood.Guidance for the utility of linear models in meta-analysis of genetic association studies of binary phenotypes.Ageing with elegans: a research proposal to map healthspan pathways.Improved imputation accuracy of rare and low-frequency variants using population-specific high-coverage WGS-based imputation reference panel.C-reactive protein upregulates the whole blood expression of CD59 - an integrative analysis.Metabolites of milk intake: a metabolomic approach in UK twins with findings replicated in two European cohorts.Challenges in understanding common disease.Personal control of privacy and data: Estonian experience.Risk of psychiatric illness from advanced paternal age is not predominantly from de novo mutations.

P2860

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P2860

Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.

http://www.wikidata.org/entity/Q34039854

description

2014 nî lūn-bûn

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2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած

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2014 թվականի փետրվարին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.

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Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.

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Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.

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Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.

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Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.

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Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.

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Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.

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P1433

International Journal of Epidemiology

P1476

Cohort Profile: Estonian Biobank of the Estonian Genome Center, University of Tartu.

@en

P2093

Harold Snieder

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Helene Alavere

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Liis Leitsalu

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Mari-Liis Tammesoo

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Pauline C Ng

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Toomas Haller

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P2860

Genetic structure of Europeans: a view from the North-East

Meta-analysis of genome-wide association studies identifies common variants in CTNNA2 associated with excitement-seeking.

Genome-wide association analyses identify 18 new loci associated with serum urate concentrations

Epidemiology of the human circadian clock

Genome-wide association study identifies multiple loci influencing human serum metabolite levels

Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study

Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes

Combined analysis of genome-wide association studies for Crohn disease and psoriasis identifies seven shared susceptibility loci

Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture

Early Ceremonial Constructions at Ceibal, Guatemala, and the Origins of Lowland Maya Civilization

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1137-1147

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scholarly article

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10.1093/IJE/DYT268

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4

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44

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Andres Metspalu

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2014-02-11T00:00:00Z

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260149111

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24518929

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P921